Canonical Allele Identifier: CA1608612304
Gene: DSP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.7584831G= , CM000668.2:g.7584831G= GRCh38
NC_000006.11:g.7585064G= , CM000668.1:g.7585064G= GRCh37
NC_000006.10:g.7530063G= NCBI36
NG_008803.1:g.48195G= , LRG_423:g.48195G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000710359.1:c.6240G= ENSP00000518230.1:p.Lys2080=
ENST00000379802.8:c.7569G= MANE Select ENSP00000369129.3:p.Lys2523=
ENST00000379802.7:c.7569G= ENSP00000369129.3:p.Lys2523=
ENST00000418664.2:c.5772G= ENSP00000396591.2:p.Lys1924=
NM_001008844.1:c.5772G= NP_001008844.1:p.Lys1924=
NM_004415.2:c.7569G= , LRG_423t1:c.7569G= NP_004406.2:p.Lys2523=
XM_011514323.1:c.6240G= XP_011512625.1:p.Lys2080=
NM_001008844.2:c.5772G= NP_001008844.1:p.Lys1924=
NM_001319034.1:c.6240G= NP_001305963.1:p.Lys2080=
NM_004415.3:c.7569G= NP_004406.2:p.Lys2523=
NM_004415.4:c.7569G= MANE Select NP_004406.2:p.Lys2523=
NM_001008844.3:c.5772G= NP_001008844.1:p.Lys1924=
NM_001319034.2:c.6240G= NP_001305963.1:p.Lys2080=